Spinal implant system and method

ABSTRACT

An interspinous implant comprises a first member and a second member. The members define a pathway. A third member is movable along the pathway relative to the first member and the second member. Systems and methods are disclosed.

TECHNICAL FIELD

The present disclosure generally relates to medical devices for thetreatment of musculoskeletal disorders, and more particularly to asurgical system that includes a spinal implant and method for treating aspine.

BACKGROUND

Spinal disorders such as degenerative disc disease, disc herniation,osteoporosis, spondylolisthesis, stenosis, scoliosis and other curvatureabnormalities, kyphosis, tumor, and fracture may result from factorsincluding trauma, disease and degenerative conditions caused by injuryand aging. Spinal disorders typically result in symptoms including pain,nerve damage, and partial or complete loss of mobility. For example,after a disc collapse, severe pain and discomfort can occur due to thepressure exerted on nerves and the spinal column.

Non-surgical treatments, such as medication, rehabilitation and exercisecan be effective, however, may fail to relieve the symptoms associatedwith these disorders. Surgical treatment of these spinal disordersincludes decompression, discectomy, laminectomy, laminoplasty, fusion,fixation and implantable prosthetics. For example, spinal stabilizationtreatments may employ implants, which may include interbody devices,plates and bone fasteners to stabilize vertebrae and facilitate healing.This disclosure describes an improvement over these technologies.

SUMMARY

In one embodiment, an interspinous implant is provided. The interspinousimplant comprises a first member and a second member. The members definea pathway. A third member is movable along the pathway relative to thefirst member and the second member. In some embodiments, systems andmethods are provided.

BRIEF DESCRIPTION OF THE DRAWINGS

The present disclosure will become more readily apparent from thespecific description accompanied by the following drawings, in which:

FIG. 1 is a perspective view of components of one embodiment of asurgical system in accordance with the principles of the presentdisclosure;

FIG. 2 is a perspective view of the components shown in FIG. 1 withparts separated;

FIG. 3 is a side view of the components shown in FIG. 1 and vertebrae;

FIG. 4 is a plan view of the components shown in FIG. 1;

FIG. 5 is a plan view of the components shown in FIG. 1;

FIG. 6 is a plan view of components of one embodiment of a surgicalsystem in accordance with the principles of the present disclosuredisposed with vertebrae;

FIG. 7 is a side view of the components and vertebrae shown in FIG. 6;

FIG. 8 is an enlarged view of he components and vertebrae shown in FIG.7;

FIG. 9 is an axial view of components of one embodiment of a surgicalsystem in accordance with the principles of the present disclosuredisposed with vertebrae;

FIG. 10 is a side view of components of the components and vertebraeshown in FIG. 9;

FIG. 11 is a plan view of components of one embodiment of a surgicalsystem in accordance with the principles of the present disclosuredisposed with vertebrae;

FIG. 12 is a perspective view of components of one embodiment of asurgical system in accordance with the principles of the presentdisclosure;

FIG. 13 is a side view of components of one embodiment of a surgicalsystem in accordance with the principles of the present disclosuredisposed with vertebrae;

FIG. 14 is a plan view of the components and vertebrae shown in FIG. 13;

FIG. 15 is an axial view of the components and vertebrae shown in FIG.13;

FIG. 16 is a perspective view of components of one embodiment of asurgical system in accordance with the principles of the presentdisclosure;

FIG. 17 is a side view of the components shown in FIG. 16; and

FIG. 18 is a side view of the components shown in FIG. 16.

DETAILED DESCRIPTION

The exemplary embodiments of the surgical system and related methods ofuse disclosed are discussed in terms of medical devices for thetreatment of musculoskeletal disorders and more particularly, in termsof a surgical system including a spinal implant and a method fortreating a spine. In some embodiments, the systems and methods of thepresent disclosure are employed with a spinal joint fusion, for example,with a cervical, thoracic, lumbar and/or sacral region of a spine. Insome embodiments, the spinal implant includes an interbody device,interspinous implant and/or bone fasteners. In some embodiments, thesystems and methods of the present disclosure are employed withdecompression, discectomy, laminectomy, laminoplasty, fusion, fixationand implantable prosthetic procedures.

In some embodiments, the surgical system includes a spinal implantcomprising a facet fixation interspinous process implant. In someembodiments, the surgical system includes a spinal implant comprising afixation implant having a curved surface to conform to the spinousprocess and provide a stable implant. In some embodiments, the spinalimplant includes openings for disposal of screws. In some embodiments,the screws are placed through the facet joints at angles that are stableand offer less risk to adjacent neural structures.

In some embodiments, the surgical system includes a spinal implantcomprising an interspinous spacer having outer portions and anintermediate portion. In some embodiments, the surgical system includesa spinal implant comprising an interspinous spacer having outer portionsand an intermediate, movable portion. In some embodiments, theintermediate portion is a central movable portion that is translatablerelative to the outer portions. In some embodiments, the outer portionsinclude screw holes. In some embodiments, the outer portions comprisewings that include screw holes. In some embodiments, the central portionof the implant is configured for translation in a cranial-caudaldirection relative to the outer portions to conform to the patientanatomy at one or more vertebral levels. In some embodiments, one ormore of the outer portions include a bump stop to resist and/or preventthe intermediate portion from sliding entirely out of the track of theouter portions. In some embodiments, a medial surface of each of theouter portions includes a groove disposed for clearance with an inferiorlamina. In some embodiments, the intermediate portion mates with aninferior spinous process more posterior than the superior spinousprocess such that an inferior surface of the spacer does not projectinside the spinal canal. In some embodiments, one or more of the outerportions include a mating element that matingly engages a mating elementof the intermediate portion to resist and/or prevent non-desirableassembly orientation of the portions of the spinal implant.

In some embodiments, the surgical system includes a spinal implantcomprising an anatomical curve and a bottom surface that is contoured tomatch and/or mate with anatomy. In some embodiments, the surgical systemincludes a spinal implant having a plate comprising an anatomicalcontour surface that engages flush with a patient anatomy to providestability and an effective screw trajectory.

In some embodiments, the surgical system includes a spinal implantcomprising a lamina notch. In some embodiments, the lamina notchfacilitates engagement of the spinal implant with a spinousprocess/laminar intersection. In some embodiments, the spinal implantincludes an inferior portion and/or a foot configured to providestability when disposed with an inferior lamina. In some embodiments,the spinal implant comprises a superior notch of one or more of themember. In some embodiments, the spinal implant comprises a notch on asuperior surface of the intermediate portion and an inferior notch thatprovide for stabilization and centering of the spinal implant withspinous processes.

In some embodiments, the surgical system includes a spinal implantcomprising openings, such as, for example, screw holes. In someembodiments, the screw holes are disposed at an angular orientation. Insome embodiments, the angular orientation is 40 degrees. In someembodiments, the screw holes comprise insertion holes. In someembodiments, the spinal implant includes a facet screw plate having amating curvature. In some embodiments, the spinal implant includes ascrew trajectory oriented through a facet and a pedicle. In someembodiments, the spinal implant comprises a trans-facet joint screwassembly, which includes at least one trans-facet screw trajectory. Insome embodiments, the outer portions include one or more central holesfor attachment with an implant inserter.

In some embodiments, the surgical system includes a spinal implantcomprising a modular plate. In some embodiments, the plate includes amiddle interspinous portion. In some embodiments, the interspinousportion is modular. In some embodiments, the plate is adjustable toconform to a patient anatomy. In some embodiments, the spinal implantincludes a plurality of interspinous portions having alternate heightsand widths to conform and/or adjust to a patient anatomy. In someembodiments, the interspinous portion is movable relative to the screwholes to accommodate a patient anatomy at different spinal levels. Insome embodiments, the interspinous portion optimizes an implant plateheight and width and the screw trajectory for each spinal level.

The present disclosure may be understood more readily by reference tothe following detailed description of the embodiments taken inconnection with the accompanying drawing figures, which form a part ofthis disclosure. It is to be understood that this application is notlimited to the specific devices, methods, conditions or parametersdescribed and/or shown herein, and that the terminology used herein isfor the purpose of describing particular embodiments by way of exampleonly and is not intended to be limiting. Also, in some embodiments, asused in the specification and including the appended claims, thesingular forms “a,” “an,” and “the” include the plural, and reference toa particular numerical value includes at least that particular value,unless the context dearly dictates otherwise. Ranges may be expressedherein as from “about” or “approximately” one particular value and/or to“about” or “approximately” another particular value. When such a rangeis expressed, another embodiment includes from the one particular valueand/or to the other particular value. Similarly, when values areexpressed as approximations, by use of the antecedent “about,” it willbe understood that the particular value forms another embodiment. It isalso understood that all spatial references, such as, for example,horizontal, vertical, top, upper, lower, bottom, left and right, are forillustrative purposes only and can be varied within the scope of thedisclosure. For example, the references “upper” and “lower” are relativeand used only in the context to the other, and are not necessarily“superior” and “inferior”.

As used in the specification and including the appended claims,“treating” or “treatment” of a disease or condition refers to performinga procedure that may include administering one or more drugs to apatient (human, normal or otherwise or other mammal), employingimplantable devices, and/or employing instruments that treat thedisease, such as, for example, micro discectomy instruments used toremove portions bulging or herniated discs and/or bone spurs, in aneffort to alleviate signs or symptoms of the disease or condition.Alleviation can occur prior to signs or symptoms of the disease orcondition appearing, as well as after their appearance. Thus, treatingor treatment includes preventing or prevention of disease or undesirablecondition (e.g., preventing the disease from occurring in a patient, whomay be predisposed to the disease but has not yet been diagnosed ashaving it). In addition, treating or treatment does not require completealleviation of signs or symptoms, does not require a cure, andspecifically includes procedures that have only a marginal effect on thepatient. Treatment can include inhibiting the disease, e.g., arrestingits development, or relieving the disease, e.g., causing regression ofthe disease. For example, treatment can include reducing acute orchronic inflammation; alleviating pain and mitigating and inducingre-growth of new ligament, bone and other tissues; as an adjunct insurgery; and/or any repair procedure. Also, as used in the specificationand including the appended claims, the term “tissue” includes softtissue, muscle, ligaments, tendons, cartilage and/or bone unlessspecifically referred to otherwise.

The following discussion includes a description of a surgical system andrelated methods of employing the surgical system in accordance with theprinciples of the present disclosure. Alternate embodiments are alsodisclosed. Reference is made in detail to the exemplary embodiments ofthe present disclosure, which are illustrated in the accompanyingfigures. Turning to FIGS. 1-5, there are illustrated components of asurgical system, such as, for example, a spinal implant system 10.

The components of spinal implant system 10 can be fabricated frombiologically acceptable materials suitable for medical applications,including metals, synthetic polymers, ceramics and bone material and/ortheir composites. For example, the components of spinal implant system10, individually or collectively, can be fabricated from materials suchas stainless steel alloys, commercially pure titanium, titanium alloys,Grade 5 titanium, super-elastic titanium alloys, cobalt-chrome alloys,stainless steel alloys, superelastic metallic alloys (e.g., Nitinol,super elasto-plastic metals, such as GUM METAL®), ceramics andcomposites thereof such as calcium phosphate (e.g., SKELITE™),thermoplastics such as polyaryletherketone (PAEK) includingpolyetheretherketone (PEEK), polyetherketoneketone (PEKK) andpolyetherketone (PEK), carbon-PEEK composites, PEEK-BaSO₄ polymericrubbers, polyethylene terephthalate (PET), fabric, silicone,polyurethane, silicone-polyurethane copolymers, polymeric rubbers,polyolefin rubbers, hydrogels, semi-rigid and rigid materials,elastomers, rubbers, thermoplastic elastomers, thermoset elastomers,elastomeric composites, rigid polymers including polyphenylene,polyamide, polyimide, polyetherimide, polyethylene, epoxy, bone materialincluding autograft, allograft, xenograft or transgenic cortical and/orcorticocancellous bone, and tissue growth or differentiation factors,partially resorbable materials, such as, for example, composites ofmetals and calcium-based ceramics, composites of PEEK and calcium basedceramics, composites of PEEK with resorbable polymers, totallyresorbable materials, such as, for example, calcium based ceramics suchas calcium phosphate such as hydroxyapatite (HA), corraline HA, biphasiccalcium phosphate, tricalcium phosphate, or fluorapatite, tri-calciumphosphate (TCP), HA-TCP, calcium sulfate, or other resorbable polymerssuch as polyaetide, polyglycolide, polytyrosine carbonate,polycaroplaetohe and their combinations, biocompatible ceramics,mineralized collagen, bioactive glasses, porous metals, bone particles,bone fibers, morselized bone chips, bone morphogenetic proteins (BMP),such as BMP-2, BMP-4, BMP-7, rhBMP-2, or rhBMP-7, demineralized bonematrix (DBM), transforming growth factors (TGF, e.g., TGF-β), osteoblastcells, growth and differentiation factor (GDF), insulin-like growthfactor 1, platelet-derived growth factor, fibroblast growth factor, orany combination thereof.

Various components of spinal implant system 10 may have materialcomposites, including the above materials, to achieve various desiredcharacteristics such as strength, rigidity, elasticity, compliance,biomechanical performance, durability and radiolucency or imagingpreference. The components of spinal implant system 10, individually orcollectively, may also be fabricated from a heterogeneous material suchas a combination of two or more of the above-described materials. Thecomponents of spinal implant system 10 may be monolithically formed,integrally connected or include fastening elements and/or instruments,as described herein. In one embodiment, a spinal implant, as describedherein, may be formed substantially of a biocompatible metal, such astitanium and selectively coated with a bone-growth promoting material,such as HA. In one embodiment, a spinal implant, as described herein,may be formed substantially of a biocompatible polymer, such as PEEK,and selectively coated with a biocompatible metal, such as titanium, ora bone-growth promoting material, such as HA. In some embodiments,titanium may be plasma sprayed onto surfaces of the spinal implant tomodify a radiographic signature of the spinal implant and/or improvebony ongrowth to the spinal implant by application of a porous orsemi-porous coating of titanium.

Spinal implant system 10 may be employed, for example, with minimallyinvasive procedures, including percutaneous techniques, mini-opensurgical techniques and/or open surgical techniques to deliver andintroduce instrumentation and/or spinal implants, such as, for example,an interspinous implant at a surgical site within a body of a patient,which includes, for example, vertebrae. One or more of the components ofsurgical system 10 including an interspinous implant can be employed,for example, in decompression, discectomy, laminectomy, laminoplasty,fusion, fixation and implantable prosthetic procedures to treat patientssuffering from a spinal disorder to provide stabilization anddecompression. In some embodiments, one or more of the components ofspinal implant system 10 is employed with a method for implanting aninterspinous process spacer between two adjacent vertebrae, whichincludes introducing the interspinous spacer adjacent a superior and aninferior spinous processes,

Spinal implant system 10 includes an interspinous implant, such as, forexample, a plate 12. In some embodiments, plate 12 is modular andcomprises end members, as described herein, to facilitate selectiveadjustability with a patient anatomy. In some embodiments, one or moreof the components and/or portions of plate 12 may have variouscross-section configurations, such as, for example, flat, cylindrical,oval, oblong, triangular, rectangular, square, polygonal, irregular,uniform, non-uniform, variable and/or tapered. In some embodiments, oneor more of the components and/or the overall geometry of plate 12 mayhave various configurations, such as, for example, oval, oblong,triangular, rectangular, square, polygonal, irregular, uniform,non-uniform, variable and/or tapered. Plate 12 defines a longitudinalaxis X1.

Plate 12 includes an end member 14, which includes an anterior surface16 and a posterior surface 18. Surface 16 is configured to engagetissue, such as, for example, vertebrae, as described herein. End member14 includes an end surface 20. In some embodiments, surface 20 includesan undulating profile. In some embodiments, surface 20 may havealternate configurations, such as, for example, arcuate, irregular,uniform, non-uniform, variable and/or tapered. Surface 20 extendsbetween surfaces 16, 18.

End member 14 includes a tissue engaging surface 22 engageable withvertebrae. In some embodiments, surface 22 includes an undulatingprofile. In some embodiments, all or a portion of surface 22 may havealternate configurations, such as, for example, arcuate, irregular,uniform, non-uniform, variable and/or tapered. Surface 22 extendsbetween surfaces 16, 18. End member 14 includes a surface 24 configuredfor engagement with tissue, such as, for example, a spinous process. Insome embodiments, surface 24 includes an angled profile. In someembodiments, surface 24 may have alternate configurations, such as, forexample, arcuate, irregular, uniform, non-uniform, variable and/ortapered. Surface 24 extends between surface 16, 18. In some embodiments,surfaces 22, 24 may be rough, textured, porous, semi-porous, dimpled,knurled, toothed, grooved and/or polished to facilitate engagement withtissue.

End member 14 includes a surface 30 that defines a slot 32 having anarcuate configuration. Slot 32 defines a portion of a pathway, such as,for example, a track 34, as described herein. Slot 32 is configured fordisposal of an intermediate member 90, as described herein, and surface30 is engageable with intermediate member 90 in a keyed connection.Surface 30 includes a retention member, such as, for example, opposingflanges 36 disposed along slot 32 and configured to engage a portion ofintermediate member 90 to retain intermediate member 90 with end member14. As intermediate member 90 translates relative to end member 14,flanges 36 retain intermediate member 90 with end member 14.

End member 14 includes an inner surface 40 that defines opening 42. Insome embodiments, opening 42 is oriented along a direct facet-pediclepathway 44, as shown in FIGS. 9 and 10. In some embodiments, opening 42is oriented along a direct posterior-anterior pathway. In someembodiments, opening 42 is oriented along a pathway aligned with a planedisposed in substantially parallel relation to a sagittal plane ofvertebrae. Pathway 44 is configured for disposal of a fastener 46, asdescribed herein. In some embodiments, pathway 44 is disposed at anangular range α relative to axis X1, as shown in FIGS. 8 and 10. In someembodiments, angular range α includes an angle in a range of 0 to 40degrees relative to axis X1.

Plate 12 includes an end member 50, which includes an anterior surface52 and a posterior surface 54. Surface 52 is configured to engagetissue, such as, for example, vertebrae, as described herein. End member50 includes a surface, such as, for example, an end surface 56. In someembodiments, surface 56 includes an undulating profile. In someembodiments, surface 56 may have alternate configurations, such as, forexample, arcuate, irregular, uniform, non-uniform, variable and/ortapered. Surface 56 extends between surfaces 52, 54.

End member 50 includes a tissue engaging surface 58 engageable withvertebrae. In some embodiments, surface 58 includes an undulatingprofile. In some embodiments, surface 58 may have alternateconfigurations, such as, for example, arcuate, irregular, uniform,non-uniform, variable and/or tapered. Surface 58 extends betweensurfaces 52, 54. End member 50 includes a surface 60 configured forengagement with tissue, such as, for example, a spinous process. In someembodiments, surface 60 includes an angled profile. In some embodiments,surface 60 may have alternate configurations, such as, for example,arcuate, irregular, uniform, non-uniform, variable and/or tapered.Surface 60 extends between surfaces 52, 54. In some embodiments,surfaces 58, 60 may be rough, textured, porous, semi-porous, dimpled,knurled, toothed, grooved and/or polished to facilitate engagement withtissue.

End member 50 includes a surface 66 that defines a slot 68 having anarcuate configuration. Slot 68 defines a portion of track 34. Slot 68 isconfigured for disposal of an intermediate member 90, as describedherein, and surface 66 is engageable with intermediate member 90 in akeyed connection. Slot 68 includes a retention member, such as, forexample, opposing flanges 70 disposed along slot 68 and configured toengage a portion of intermediate member 90 to retain intermediate member90 with end member 50. As intermediate member 90 translates relative toend member 50, flanges 70 retain intermediate member 90 with end member50.

End member 50 includes an inner surface 72 that defines opening 74. Insome embodiments, opening 74 is oriented along a direct facet-pediclepathway 76, as shown in FIGS. 9 and 10. In some embodiments, opening 74is oriented along a direct posterior-anterior pathway. In someembodiments, opening 74 is oriented along a pathway aligned with a planedisposed in substantially parallel relation to a sagittal plane ofvertebrae. In some embodiments, pathway 76 is disposed at an angularrange α relative to axis X1 similar to pathway 44.

Intermediate member 90 is configured for movable disposal within slots32, 68 along track 34 for selective adjustability of plate 12 with apatient anatomy and/or positioning for attachment and/or implantationwith tissue. Track 34 facilitates translation of intermediate member 90relative to end members 14, 50 along a cranial-caudal trajectory, asshown by arrows A in FIG. 2, for selective adjustment to engagevertebrae and/or orient an openings 42, 74, as described herein. In someembodiments, intermediate member 90 is translatable relative to endmembers 14, 50 to facilitate engagement with vertebrae, as describedherein. In some embodiments, intermediate member 90 is translatablealong track 34 in a range of slidable movement relative to end members14, 50 between a superior vertebral limit, as shown in FIG. 4, and aninferior vertebral limit, as shown in FIG. 5.

In some embodiments, intermediate member 90 is translatable along track34 relative to openings 42, 74 to facilitate engagement of fasteners 46with vertebrae, such as, for example, facets/pedicles and accommodatevariation in patient anatomies and/or different spinal levels of apatient. In some embodiments, end member 14 is movable relative to endmember 50 and/or intermediate member 90. In some embodiments, end member50 is movable relative to end member 14 and/or intermediate member 90.

Intermediate member 90 is configured to connect end member 14 with endmember 50 to form a modular plate 12 to facilitate selectiveadjustability of plate 12 relative to adjacent vertebrae. In someembodiments, surgical system 10 comprises a kit including a plurality ofalternate intermediate members 90 having varying width and/or height tofacilitate engagement with varied patient anatomy. Intermediate member90 includes an anterior surface 92 and a posterior surface 94.Intermediate member 90 extends between an end 96 and an end 98.

Surface 94 includes a protrusion 100. Protrusion 100 extends between anend 102 and an end 104. Protrusion 100 extends a distance from surface94 and is configured for disposal between vertebrae, such as, forexample, spinous process’. In some embodiments protrusion 100 comprisesa handle to facilitate translation of intermediate member 90 and/orpositioning of plate 12.

End 102 includes a surface 106 engageable with vertebrae, such as, forexample, a spinous process and/or a lamina/spinous process intersection.End 104 includes a surface 108 engageable with vertebrae, such as, forexample, a spinous process and/or a lamina/spinous process intersection.End 104 includes an arcuate portion 110 engageable with vertebrae andcontoured to a shape of a spinous process.

Intermediate member 90 includes an edge, such as, for example, a keyedportion 112 disposable with slot 32 during translation of intermediatemember 90 relative to member 14. Portion 112 includes an enlargedportion 114 that extends between ends 96, 98. Portion 114 is disposedwith slot 32 and engageable with opposing flanges 36 in a movably lockedorientation with member 14 to retain and prevent removal of intermediatemember 90 from slot 32 during relative translation. Intermediate member90 includes an edge, such as, for example, a keyed portion 120disposable with slot 68 during translation of intermediate member 90relative to member 50. Portion 120 includes an enlarged portion 122 thatextends between ends 96, 98. Portion 122 is disposed with slot 68 andengageable with opposing flanges 70 in a movably locked orientation withmember 50 to retain and prevent removal of intermediate member 90 fromslot 68 during relative translation.

Surfaces 22, 106, 58 define a cavity 124. Cavity 124 is configured fordisposal of vertebrae, such as, for example, a spinous process and/or alamina/spinous process intersection. In some embodiments, cavity 124 isarcuate in shape. In some embodiments, cavity 124 may have alternateconfigurations, such as, for example, irregular, uniform, non-uniform,variable and/or tapered. In some embodiments, the configuration anddimension of cavity 124 is adjustable via translation of intermediatemember 90 relative to end members 14, 50.

Surfaces 24, 108, 60 define a cavity 128. Cavity 128 is configured fordisposal of vertebrae, such as, for example, a spinous process and/or alamina/spinous process intersection. In some embodiments, cavity 128includes a trapezoid profile. In some embodiments, cavity 128 may havealternate configurations, such as, for example, angled, arcuate,irregular, uniform, non-uniform, variable and/or tapered. In someembodiments, the configuration and dimension of cavity 128 is adjustablevia translation of intermediate member 90 relative to end members 14,50.

Surfaces 16, 52, 92 define a tissue mating curvature 130 of plate 12, asshown in FIG. 3. Curvature 130 includes a profile P1 that matches and/ormates with a profile P2 of vertebrae V. As such, curvature 130 isconfigured for selective engagement with vertebrae, such as, forexample, a spinous process, lamina, tissue adjacent a lamina/spinousand/or tissue adjacent facet joints. In some embodiments, curvature 130includes an undulating profile. In some embodiments, curvature 130 isadjustable via translation of intermediate member 90 relative to endmembers 14, 50.

For example, curvature 130 is contoured and engages flush with tissue tomate profile P1 with profile P2 of vertebrae V such that plate 12conforms with the anatomy of adjacent facet joints FJ1, FJ2 and/or otheradjacent tissue. Curvature 130 facilitates stability between plate 12and vertebrae. In some embodiments, curvature 130 may have alternateconfigurations, such as, for example, arcuate, irregular, uniform,non-uniform, variable and/or tapered. In some embodiments, profile P1mates with profile P2 to provide stability and an effective screwtrajectory,

In assembly, operation and use, surgical system 10, similar to thesystems and methods described herein, is employed to treat a selectedsection of vertebrae V, as shown in FIGS. 6-10. A medical practitionerobtains access to a surgical site including vertebrae V in anyappropriate manner, such as through incision and retraction of tissues.In some embodiments, surgical system 10 can be used in any existingsurgical method or technique including open surgery, mini-open surgery,minimally invasive surgery and percutaneous surgical implantation,whereby vertebrae V is accessed through a mini-incision, or sleeve thatprovides a protected passageway to the area. Once access to the surgicalsite is obtained, the particular surgical procedure can be performed fortreating a spine disorder. In some embodiments, one or all of thecomponents of surgical system 10 can be delivered or implanted as apre-assembled device or can be assembled in situ. The components ofsurgical system 10 may be completely or partially revised, removed orreplaced.

An incision is made in the body of a patient and a cutting instrument(not shown) creates a surgical pathway for implantation of components ofsurgical system 10 with a portion of vertebrae V including spinousprocess SP1, spinous process SP2, facet joint FJ1 and facet joint FJ2. Apreparation instrument (not shown) can be employed to prepare tissuesurfaces of vertebrae V, as well as for aspiration and irrigation of asurgical region.

Pilot holes are made in vertebrae V1, V2 for receiving fixationelements, such as, for example, fasteners 46. Pilot holes are orientedalong facet-pedicle pathways 44, 76, as described herein. Plate 12, asdescribed herein, is delivered and introduced to the surgical siteadjacent spinous process SP1, spinous process SP2, facet joint FA andfacet joint FJ2. Spinous process SP1 is disposed with cavity 124 andspinous process SP2 is disposed with cavity 128,

Intermediate member 90 and end members 14, 50 are slidably andselectively adjusted, as described herein, such that plate 12 conformsto the anatomy of spinous process SP1, spinous process SP2, facet jointFJ1 and facet joint FJ2. Intermediate member 90 is translated relativeto end members 14, 50 along track 34 and a cranial-caudal trajectory, asshown by arrows A in FIG. 6.

Surface 106 engages spinous process SP1 and surface 108 engages spinousprocess SP2. This configuration provides for selective adjustment ofplate 12 to engage vertebrae and orient openings 42, 74, as describedherein. Intermediate member 90 and end members 14, 50 are slidably andselectively adjusted to align openings 42, 74 with the pilot holes toaccommodate variation in anatomy at different vertebral levels.Fasteners 46 are disposed with openings 42, 74 and engaged withvertebrae V to fasten plate 12 with vertebrae V1, V2.

Upon selective orientation of plate 12 with the anatomy of spinousprocess SP1, spinous process SP2, facet joint FJ1 and facet joint FJ2,curvature 130 engages flush with tissue to mate profile P1 with profileP2, as described herein. Plate 12 conforms with the anatomy of spinousprocess SP1, spinous process SP2, facet joint FJ1 and facet joint FJ2,and/or adjacent tissue.

In one embodiment, as shown in FIG. 11, spinal implant system 10comprises a kit including a plurality of alternate interspinous implantscomprising a plurality of modular plates 12, similar to that describedherein. The modular plates 12 can be of alternate configuration anddimension and include end members 14, 50 described herein, and one of aplurality of alternately configured and dimensioned intermediate members90a, 90b, similar to intermediate member 90 described herein. A superiororiented plate 12 includes intermediate member 90a having a smallerwidth to conform with the anatomy of vertebrae V1, V2, similar to thatdescribed herein. An inferior oriented plate 12 includes intermediatemember 90b having a larger width to conform with the anatomy ofvertebrae V2, V3, similar to that described herein.

In some embodiments, spinal implant system 10 can include one or aplurality of fasteners such as those described herein and/or fixationelements, which may be employed with a single vertebral level or aplurality of vertebral levels. In some embodiments, fasteners 46 may beengaged with vertebrae in various orientations, such as, for example,series, parallel, offset, staggered and/or alternate vertebral levels.In some embodiments, fasteners 46 may be configured as multi-axialscrews, sagittal angulation screws, pedicle screws, mono-axial screws,uniplanar screws, fixed screws, anchors, tissue penetrating screws,conventional screws, expanding screws. In some embodiments, fasteners 46may be employed with wedges, anchors, buttons, clips, snaps, frictionfittings, compressive fittings, expanding rivets, staples, nails,adhesives, posts, connectors, fixation plates and/or posts.

In one embodiment, spinal implant system 10 includes an agent, which maybe disposed, packed, coated or layered within, on, adjacent or about thecomponents and/or surfaces of spinal implant system 10, and/or disposedwith tissue. In some embodiments, the agent may include bone growthpromoting material, such as, for example, bone graft to enhance fixationof the components and/or surfaces of spinal implant system 10 withvertebrae. In some embodiments, the agent may include one or a pluralityof therapeutic agents and/or pharmacological agents for release,including sustained release, to treat, for example, pain, inflammationand degeneration.

Upon completion of a procedure, as described herein, the surgicalinstruments, assemblies and non-implanted components of spinal implantsystem 10 are removed and the incision(s) are closed. One or more of thecomponents of spinal implant system 10 can be made of radiolucentmaterials such as polymers. Radiopaque markers may be included foridentification under x-ray, fluoroscopy, CT or other imaging techniques.In some embodiments, the use of surgical navigation, microsurgical andimage guided technologies may be employed to access, view and repairspinal deterioration or damage, with the aid of spinal implant system10,

In one embodiment, as shown in FIGS. 12-15, spinal implant system 10,similar to the systems and methods described herein, includes a plate212, similar to plate 12 described herein. Plate 212 defines alongitudinal axis X2. Plate 212 includes an end member 214, whichincludes an anterior surface 216 and a posterior surface 218. Surface216 is configured to engage spinous process SP1, spinous process SP2,facet joint FJ1, facet joint FJ2 and/or adjacent tissue, similar tosurface 16 described herein. End member 214 includes an end surface 220that extends between surfaces 216, 218.

End member 214 includes a tissue engaging surface 222 engageable withspinous process SP1 and extending between surfaces 216, 218. End member214 includes a surface 224 configured for engagement with spinousprocess SP2. Surface 224 extends between surface 216, 218. In someembodiments, surfaces 222, 224 may be rough, textured, porous,semi-porous, dimpled, knurled, toothed, grooved and/or polished tofacilitate engagement with tissue.

End member 214 includes an inner surface 240 that defines an opening242, similar to opening 42 described herein, which is oriented along apathway, similar to pathway 44 described herein.

Plate 212 includes an end member 250, which includes an anterior surface252 and a posterior surface 254. Surface 252 is configured to engagespinous process SP1, spinous process SP2, facet joint RP, facet jointFJ2 and/or adjacent tissue, similar to surface 52 described herein. Endmember 250 includes an end surface 256 that extends between surfaces252, 254.

End member 250 includes a tissue engaging surface 258 engageable withspinous process SP1 and extending between surfaces 252, 254. End member250 includes a surface 260 configured for engagement with spinousprocess SP2 and extending between surfaces 252, 254. In someembodiments, surfaces 258, 260 may be rough, textured, porous,semi-porous, dimpled, knurled, toothed, grooved and/or polished tofacilitate engagement with tissue.

End member 250 includes an inner surface 272 that defines opening 274,similar to opening 74 described herein, which is oriented along apathway, similar to pathway 76 described herein.

An intermediate member 290 connects and is monolithically formed withend members 214, 250. Intermediate member 290 includes an anteriorsurface 292 and a posterior surface 294. Intermediate member 290 extendsbetween an end 296 and an end 298. Surfaces 222, 296, 258 define acavity 324. Cavity 324 is configured for disposal of spinous processSP1. Surfaces 224, 298, 260 define a cavity 328. Cavity 328 isconfigured for disposal of spinous process SP2.

Surfaces 216, 252, 292 define a tissue mating curvature 330, similar tocurvature 130 described herein. Curvature 330 includes a profile thatmatches and/or mates with a profile of vertebrae V, as shown in FIG. 13.For example, curvature 330 is contoured and engages flush with tissue tomate with vertebrae V such that plate 212 conforms with the anatomy ofadjacent facet joints FJ1, FJ2 and/or other adjacent tissue. Curvature330 facilitates stability between plate 212 and vertebrae. In someembodiments, curvature 330 includes an inferior portion and/or a footconfigured to provide stability when disposed with an inferior lamina.

In one embodiment, as shown in FIGS. 16-18, spinal implant system 10,similar to the systems and methods described herein, includes a plate412, similar to plate 12 described herein. In some embodiments, plate412 is modular and comprises end members, as described herein, tofacilitate selective adjustability with a patient anatomy. Plate 412defines a longitudinal axis X3.

Plate 412 includes an end member 414, which includes an anterior surface416 and a posterior surface 418. Surface 416 is configured to engagetissue, such as, for example, vertebrae, as described herein. End member414 includes an end surface 420. In some embodiments, surface 420includes an undulating profile.

End member 414 includes a tissue engaging surface 422 engageable withvertebrae. End member 414 includes a surface 424 configured forengagement with tissue, such as, for example, a spinous process. In someembodiments, surface 422 and/or surface 424 can be disposed forclearance with an inferior lamina.

End member 414 includes a surface 430 that defines a slot 432. Slot 432defines a portion of a pathway, such as, for example, a track 434,similar to track 34, as described herein. Slot 432 is configured fordisposal of an intermediate member 490, as described herein. Surface 430includes opposing flanges 436 disposed along slot 432 and configured toengage a portion of intermediate member 490 to retain intermediatemember 490 with end member 414. Surface 430 includes a protrusion, suchas, for example, a bump stop 438. In some embodiments, bump stop 438resists and/or prevents intermediate member 490 from sliding entirelyout of track 434. In some embodiments, the protrusion may have variousconfigurations, such as, for example, oval, oblong, triangular,rectangular, square, polygonal, irregular, uniform, non-uniform,variable and/or tapered.

End member 414 includes an inner surface 440 that defines an opening442, similar to opening 42 described herein, configured for disposal ofa fastener, as described herein. End member 414 includes an innersurface 444 that defines a central opening 446 configured for engagementwith a surgical instrument, such as, for example, an insertion tool tofacilitate insertion of plate 412 with a surgical site.

Plate 412 includes an end member 450, which includes an anterior surface452 and a posterior surface 454. Surface 452 is configured to engagetissue, such as, for example, vertebrae, as described herein. End member450 includes an end surface 456. In some embodiments, surface 456includes an undulating profile.

End member 450 includes a tissue engaging surface 458 engageable withvertebrae. End member 450 includes a surface 460 configured forengagement with tissue, such as, for example, a spinous process. In someembodiments, surface 458 and/or surface 460 can be disposed forclearance with an inferior lamina.

End member 450 includes a surface 466 that defines a slot 468. Slot 468defines a portion of track 434. Slot 468 is configured for disposal ofintermediate member 490, as described herein. Slot 468 includes opposingflanges 470 disposed along slot 468 and configured to engage a portionof intermediate member 490 to retain intermediate member 490 with endmember 450. Surface 466 includes a protrusion, such as, for example, abump stop 471, similar to stop 438. In some embodiments, bump stop 471resists and/or prevents intermediate member 490 from sliding entirelyout of track 434,

End member 450 includes an inner surface 472 that defines opening 474,similar to opening 74 described herein, configured for disposal of afastener, as described herein. End member 450 includes an inner surface476 that defines a central opening 478 configured for engagement with asurgical instrument, such as, for example, an insertion tool tofacilitate insertion of plate 412 into a surgical site.

Intermediate member 490 is configured for movable disposal within slots432, 468 along track 434 for selective adjustability of plate 412 with apatient anatomy and/or positioning for attachment and/or implantationwith tissue, as described herein. Track 434 facilitates translation ofintermediate member 490 relative to end members 414, 450 along acranial-caudal trajectory, as described herein, for selective adjustmentto engage vertebrae and/or orient openings 442, 474, similar to thatdescribed herein. In some embodiments, intermediate member 490 istranslatable relative to end members 414, 450 to facilitate engagementwith vertebrae, as described herein. In some embodiments, intermediatemember 490 is translatable along track 434 in a range of slidablemovement relative to end members 414, 450 between a superior vertebrallimit and an inferior vertebral limit, as described herein.

Intermediate member 490 is configured to connect end member 414 with endmember 450 to form a modular plate 412 to facilitate selectiveadjustability of plate 412 relative to adjacent vertebrae, similar tothat described herein. Intermediate member 490 includes an anteriorsurface 492 and a posterior surface 494. Intermediate member 490 extendsbetween an end 496 and an end 498. In some embodiments, intermediatemember 490 mates with an inferior spinous process more posterior thanthe superior spinous process such that an inferior surface of plate 412does not project inside the spinal canal.

End 496 includes a surface 500 engageable with vertebrae, such as, forexample, a spinous process and/or a lamina/spinous process intersection.End 496 includes a portion 502 engageable with vertebrae and contouredto a shape of a spinous process. End 498 includes a surface 508engageable with vertebrae, such as, for example, a spinous processand/or a lamina/spinous process intersection. End 498 includes a portion510 engageable with vertebrae and contoured to a shape of a spinousprocess. In some embodiments, portion 502 comprises a notch on asuperior surface of intermediate member 490 and portion 510 comprises aninferior notch that provide for stabilization and centering of plate 412with spinous processes.

Intermediate member 490 includes an edge, such as, for example, a keyedportion 512, similar to portion 112, disposable with slot 432 duringtranslation of intermediate member 490 relative to member 414.Intermediate member 490 includes an edge, such as, for example, a keyedportion 520, similar to portion 120, disposable with slot 468 duringtranslation of intermediate member 490 relative to member 450.

Surfaces 422, 500, 458 define a cavity 524, similar to cavity 124,configured for disposal of vertebrae, such as, for example, a spinousprocess and/or a lamina/spinous process intersection. Surfaces 424, 508,460 define a cavity 528. Cavity 528 is configured for disposal ofvertebrae, such as, for example, a spinous process and/or alamina/spinous process intersection. Surfaces 416, 452, 492 define atissue mating curvature 530, similar to cavity 130, of plate 412, asshown in FIG. 17. Curvature 530 includes a profile that matches and/ormates with a profile of vertebrae, as described herein.

it will be understood that various modifications may be made to theembodiments disclosed herein. Therefore, the above description shouldnot be construed as limiting, but merely as exemplification of thevarious embodiments. Those skilled in the art will envision othermodifications within the scope and spirit of the claims appended hereto.

1. An interspinous implant comprising: a first member extending betweenopposite first and second ends; a second member extending betweenopposite first and second ends, the members defining a pathway thatextends from the first ends to the second ends; and a third memberextending between opposite first and second ends, the third member beingmovable along the pathway relative to the first member and the secondmember, the pathway extending from the first ends of the first andsecond members to the second ends of the first and second members,wherein the first ends define a first cavity configured for disposal ofa first spinous process and the second ends define a second cavityconfigured for disposal of a second spinous process.
 2. An interspinousimplant as recited in claim 1, wherein the members comprise a plateincluding a vertebral engaging surface that defines a tissue matingcurvature.
 3. An interspinous implant as recited in claim 2, wherein thecurvature includes an undulating profile.
 4. An interspinous implant asrecited in claim 1, wherein the members comprise a plate including ananterior surface and a posterior surface, the anterior surface defininga tissue mating curvature engageable with tissue of a facet joint. 5.(canceled)
 6. An interspinous implant as recited in claim 1, wherein atleast one of the first member and the second member includes an innersurface that defines an opening, and further comprising a trans-facetjoint fastener configured for disposal with the opening.
 7. Aninterspinous implant as recited in claim 1, wherein the members arerelatively movable and selectively adjustable to engage vertebrae.
 8. Aninterspinous implant as recited in claim 1, wherein the first member andthe second member are separate and connected via the third member.
 9. Aninterspinous implant as recited in claim 1, wherein the third member ismovable along the pathway in a cranial-caudal orientation.
 10. Aninterspinous implant as recited in claim 1, wherein the pathway includesa slot of the first member and a slot of the second member, the thirdmember including a first key movable in the slot of the first member anda second key movable in the slot of the second member.
 11. Aninterspinous implant as recited in claim 1, wherein at least one of thefirst member and the second member includes an inner surface thatdefines an opening oriented along a trans-facet fastener pathway.
 12. Aninterspinous implant as recited in claim 1, wherein the pathway includesan arcuate slot of the first member and an arcuate slot of the secondmember, the third member including enlarged edge portions locked withand movable in the slots.
 13. An interspinous implant as recited inclaim 1, wherein at least one of the first member and the second memberincludes an inner surface that defines an opening oriented along adirect posterior-anterior fastener pathway.
 14. An interspinous implantas recited in claim 1, wherein at least one of the first member and thesecond member includes an inner surface that defines an opening orientedalong a facet-pedicle fastener pathway.
 15. An interspinous implantcomprising: a first member extending between opposite first and secondends, the first member defining an opening and including an innersurface defining a slot that extends from the first end to the secondend; a second member extending between opposite first and second ends,the second member defining an opening and including an inner surfacedefining a slot that extends from the first end of the second member tothe second end of the second member, the slots defining an arcuate trackand the members including a vertebral engaging surface that defines atissue mating curvature; and an intermediate member extending betweenopposite first and second ends, the intermediate member being movablealong the track relative to the first member and the second member,wherein the first ends define a first cavity configured for disposal ofa first spinous process and the second ends define a second cavityconfigured for disposal of a second spinous process.
 16. An interspinousimplant as recited in claim 15, wherein the members are relativelymovable and selectively adjustable to engage vertebrae and/or orient theopenings.
 17. A plate comprising: a first member extending betweenopposite first and second ends, the first member including a slot thatextends from the first end to the second end; a second member extendingbetween opposite first and second ends, the second member including aslot that extends from the first end of the second member to the secondend of the second member; and an intermediate member extending betweenopposite first and second ends, the intermediate member comprising sidesurfaces that are each movably disposed within one of the slots, thefirst ends defining a first cavity configured for disposal of a firstspinous process and the second ends defining a second cavity configuredfor disposal of a second spinous process, the plate including avertebral engaging surface that defines a tissue mating curvature.
 18. Aplate as recited in claim 17, wherein the curvature includes anundulating profile.
 19. (canceled)
 20. A plate as recited in claim 17,wherein the plate defines a longitudinal axis and at least one fasteneropening being oriented in an angular range of 0 through 40 degreesrelative to the longitudinal axis.
 21. An interspinous implant asrecited in claim 1, wherein the second end of the third member comprisesan arcuate portion that defines a portion of the second cavity.
 22. Aninterspinous implant as recited in claim 15, wherein the members includea posterior surface opposite the vertebral engaging surface, theintermediate member having a protrusion that extends outwardly from theposterior surface.